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dc.contributor.authorKeskin, S.
dc.contributor.authorYildiz, I.
dc.contributor.authorSen, F.
dc.contributor.authorAydogan, F.
dc.contributor.authorKilic, L.
dc.contributor.authorEkenel, M.
dc.contributor.authorAykan, F.
dc.date.accessioned2019-08-13T12:10:23Z
dc.date.accessioned2019-08-13T16:03:10Z
dc.date.available2019-08-13T12:10:23Z
dc.date.available2019-08-13T16:03:10Z
dc.date.issued2013
dc.identifier.issn1699-048X
dc.identifier.urihttps://dx.doi.org/10.1007/s12094-012-0942-8
dc.identifier.urihttp://hdl.handle.net/11446/3016
dc.descriptionWOS: 000318290100010en_US
dc.descriptionPubMed ID: 23054756en_US
dc.description.abstractThe aim of this retrospective study (from January 2007 to December 2011) was to investigate the efficacy and tolerability of mDCF schedule for chemotherapy-na < ve AGC patients. Patients (n = 54) with locally inoperable or distant metastasis and performance status of 0-2 were eligible. The triplet combination chemotherapy consisting of docetaxel 60 mg/m(2) on day 1, cisplatin 60 mg/m(2) on day 1, and 5-fluorouracil 600 mg/m(2) for 5 days of continuous infusion were administered every 21 days, up to nine cycles. Prophylactic G-CSF was not allowed. In all, 36 (67 %) patients were male and 18 (33 %) were female; median age was 59 years. The majority of patients (n = 46, 85 %) had metastatic disease and 8 (15 %) of them had locally advanced disease. Liver metastasis and peritonitis carcinomatosa were found in 20 (43 %) and 18 (39 %) of the 46 cases, respectively. The median cycle of chemotherapy was 6. In assessing 50 patients for response evaluation, one had complete response. Partial response was achieved in 27 (54 %) patients. Seventeen patients (34 %) had stable disease and 5 (10 %) had progressive disease, while 4 % (n = 2) and 11 % (n = 6) of the patients developed severe (grade 3-4) neutropenia and anemia, respectively. During the median follow-up time (6.9 months, range 0.4-24), 28 (52 %) patients died. The overall and progression-free survival were 10.7 [95 % CI 8.9-12.4] and 6.8 [95 % CI 5.8-7.8] months, respectively. Although this was not a prospective comparative study, the mDCF regimen seems to be as effective as the original DCF in AGC with acceptable and manageable side effects.en_US
dc.language.isoengen_US
dc.publisherSPRINGERen_US
dc.identifier.doi10.1007/s12094-012-0942-8en_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.subjectModified DCFen_US
dc.subjectAdvanced gastric canceren_US
dc.subjectEfficacyen_US
dc.subjectAdverse effecten_US
dc.subjectSurvivalen_US
dc.titleModified DCF (mDCF) regimen seems to be as effective as original DCF in advanced gastric cancer (AGC)en_US
dc.typearticleen_US
dc.relation.journalCLINICAL & TRANSLATIONAL ONCOLOGYen_US
dc.departmentDBÜen_US
dc.identifier.issue5en_US
dc.identifier.volume15en_US
dc.identifier.startpage403en_US
dc.identifier.endpage408en_US
dc.contributor.authorID0000-0002-5569-0913en_US
dc.contributor.authorID0000-0002-5472-3218en_US
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.department-temp[Keskin, S. -- Yildiz, I. -- Sen, F. -- Aydogan, F. -- Kilic, L. -- Ekenel, M. -- Sakar, B. -- Aykan, F.] Istanbul Univ, Inst Oncol, Dept Med Oncol, TR-34093 Istanbul, Turkey -- [Saglam, S.] Istanbul Bilim Univ, Dept Med Oncol, Istanbul, Turkey -- [Disci, R.] Istanbul Univ, Fac Med, Dept Publ Hlth, TR-34093 Istanbul, Turkeyen_US


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